- Olympus Corporation of the Americas (Center Valley, PA)
- …more about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr. Clinical Trial Coordinator (Sr. CTC) will be responsible for ... and primary point of accountability and reconciliation for the Trial Master File (TMF) and the Investigator Site File...resolution of data queries under the guidance of the Clinical Research Associate (CRA), Data Management and/or… more
- Caris Life Sciences (Phoenix, AZ)
- …yourself, Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist-Biorepository provides operational and regulatory support for ... + Candidates should have 1-2 years' experience in a Biorepository setting or Clinical Trial setting + Proficient in Microsoft Office Suite, specifically Word,… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …manage trial progress. Medical Monitoring: Provide medical oversight during clinical trials to ensure participant safety and data integrity.Review and interpret ... OverviewThe Respiratory Clinical Development Medical Lead will oversee the clinical and medical aspects of new respiratory medicines, including new drug or… more
- Stony Brook University (Stony Brook, NY)
- …correspondence with sponsors and IRB in obtaining approvals and maintenance of clinical trial materials and documents. Experience with research informed consent ... Clinical Research Associate II **Required Qualifications...Neurosurgery clinical research trials; collect and submit clinical trial patient data, coordinate patient appointments.… more
- Jazz Pharmaceuticals (Atherton, CA)
- …of innovative, complex and transformative AI/ML/GenAI solutions across the areas of Clinical Trial Execution and Digital Healthcare across Jazz Research and ... Functions Lead the development and implementation of AI/ML/GenAI solutions to optimize clinical trial operations, including such areas as patient recruitment,… more
- BeOne Medicines (Emeryville, CA)
- …with CRAs to ensure data collection is met per contractual guidelines - Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to ... Familiar with industry CTMS and data management systems **Other Qualifications:** - Understands clinical trial processes with a thorough knowledge of ICH and… more
- Merck & Co. (Rahway, NJ)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
- Merck & Co. (Boston, MA)
- …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- Merck & Co. (Upper Gwynedd, PA)
- … Clinical Judgment, Clinical Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial Development, Communication, Data Analysis, ... serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical ...an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor,… more
- Stony Brook University (Stony Brook, NY)
- …cancer clinical trials. Incumbent will facilitate the development of robust, compliant clinical trial budgets as well as the execution of post-award tasks to ... ensure timely receipt of clinical trial revenue. The ideal candidate will...**Job Number:** 2503685 **Official Job Title:** : Project Staff Associate **Job Field** : Administrative & Professional (non- Clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- Merck & Co. (North Wales, PA)
- …Engineering or closely related field plus 9 years SAS programming experience in a clinical trial environmentOR a Master's degree (or US equivalent) in Computer ... closely related field plus 7 years SAS programming experience in a clinical trial environment.Requirements:Experience and knowledge in leading large and/or… more
- Insmed Incorporated (Minneapolis, MN)
- …strong related experience.Other Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical ... for the future of science, we're in. Are you?About the Role:The Associate Director Medical Science Liaison will develop and maintain professional relationships with… more
- Merck & Co. (Rahway, NJ)
- …field and relevant experienceRequired Experience and Skills:-- -A deep understanding of the clinical trial process: You can speak the language of protocols, ... Job DescriptionWe are seeking an Associate Principal Scientist to contribute to a pivotal...stewarding these data, you will empower our scientists and clinical teams to make faster, data-driven decisions that propel… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and globally, and provide legal support for licensing, co-promotion, co-development, clinical trial collaboration, co-marketing and acquisition agreements (among ... in negotiating, drafting and reviewing licensing, co-promotion, co-development, co-marketing, clinical trial collaboration, companion diagnostic, and acquisition… more
- Insmed Incorporated (San Diego, CA)
- …automation, development of custom tools, and data exchange solutions that enhance clinical trial efficiency.Solid understanding of CDISC standards (CDASH, SDTM) ... future of science, we're in. Are you?About the Role:The Associate Director, EDC Programming will lead and oversee EDC...and oversee EDC programming, and database build for in-house clinical trials. This role will be responsible for the… more
- Insmed Incorporated (St. Louis, MO)
- …and infectious diseaseOther Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical ... a local medical and scientific resource to Insmed for product planning, clinical insights, and intelligence. Collect, synthesize and deliver HCP derived scientific… more
- Aequor (New York, NY)
- …Supporting the development of the patient reported outcomes strategy in a clinical trial setting Literature review and evidence synthesis. Supporting ... Description: Research Associate (Contractor) HTA Value & Evidence, Oncology, Global...the development and execution of deliverables to support early clinical development programs. The position is located at Headquarters… more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …Day Shift **Purpose Statement/Position Summary:** As a certified research professional, handles clinical trial administration for all protocol phases. Serves as ... other CRCs within the department. Trains new staff. Develops procedures related to clinical trial coordination. In addition, this role supports complex … more
- Insmed Incorporated (NJ)
- … Director of Biostatistics is responsible for the statistical aspects for complex clinical trial (s) or indication product line. This role leads the protocol ... statistical section development, study setup, execution, analysis, and reporting of clinical trials, and interacts with cross-functional teams.What You'll Do: Lead… more
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